Due to our business expansion and facility growth, we are looking for a **QA Scientist for Batch release** to join our dynamic team. As QA Scietntist your responsibilities will include: * + Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products to be released. + Participate in the evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls of pharmaceutical products to be released ensuring the application of GMPs and according to the marketing authorisation or clinical trial authorisation. + Participate in the certification process of batches susceptible to be released to the market or for clinical trials. + Review of Quality/Technical Agreements between the company and manufacturers and marketing authorisation holders, especially with regard to batch certification activities. + Review and approve the documentation involved in the activity of the company: CoA, Site Master File, SOPs, product specifications. + Collaborate and participate in the revision of audit reports carried out by third\-parties to the manufacturers of pharmaceutical products to be released. + Collaborate in audits carried out by our clients and give support in the Inspections of regulatory authorities. + Participate in the implementation and improvement of the quality system of the company. **If you join us, you will become part of an agile and growing company with a strong scientific culture.** Here's what you can expect: * A collaborative, empowering environment focused on continuous learning and professional growth * Hybrid work model with flexible Hours and intensive Fridays. * A Flexible employee benefits platform. * 23 vacation days per year \+ 24th and 31st of December as holidays. * A Fully stocked kitchen (Coffee, fruits, snacks, and beverages). * An inspiring workplace surrounded by nature\- our headquarters located at the foot of Collserola Natural Park (Barcelona) with a Rooftop terrace an beautiful views **What we are looking for:** * Scientific degree in Biology, Chemistry, Pharmacy or Biotechnology * 2 years of experience in Quality Control or Manufacturing activities in Quality Assurance or Quality Control or Manufacturing in the Pharmaceutical Industry. * Experience on Biologicals will be highly valued * Proactive, organized, and client oriented mindset. * A high level of English, both written and spoken is required for this position. Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.